The Detection of Rifampin-Resistant Mycobacterium tuberculosis by Polymerase Chain Reaction and Single - Strand Conformation Polymorphism Analysis.
- Author:
Jin Woo JU
;
Hae Jung BAE
;
Jeong Nyeo LEE
- Publication Type:Original Article
- MeSH:
Humans;
Korea;
Mycobacterium tuberculosis*;
Mycobacterium*;
Nucleic Acid Conformation;
Polymerase Chain Reaction*;
Rifampin;
Tuberculosis
- From:Journal of the Korean Society for Microbiology
1997;32(4):381-388
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Control of tuberculosis is threatened by widesread emergence of drug resistant Mycobacterium tuberculosis. Rifampin is a key component among therapeutic regimens for the tuberculosis; therefore patients in whom resistance to this drug develop have a poor outlook, particularly if rifampin resistance is associated with resistance to other tuberculosis drugs. The purpose of this study was to detect the mutation in rpoB gene of rifampin resistant M. tuberculosis in Korea and to evaluate the usefulness of the method in clinical aspects. A sample of 80 M. tuberculosis was studied, and it included 40 rifampin resistance isolates and 40 rifampin sensitive isolates by conventional methods. The detection method involved the amplification by polymerase chain reaction (PCR) of the Rif' region and the identification of mutations by single-strand DNA conformation polymorphism analysis (SSCP) of the amplification products (157 bp). Mutation were identified in 39 of 40 rifampin resistant isolates, and in 1 of 40 rifampin sensitive isolates.
